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Article: Discovery of regulatory motifs in 5′ untranslated regions using interpretable multi-task learning models

TitleDiscovery of regulatory motifs in 5′ untranslated regions using interpretable multi-task learning models
Authors
Keywordseukaryotic translation
explainable AI
motif discovery
multi-task learning
sequence modeling
Issue Date20-Dec-2023
PublisherElsevier
Citation
Cell Systems, 2023, v. 14, n. 12, p. 1103-1112 How to Cite?
Abstract

The sequence in the 5′ untranslated regions (UTRs) is known to affect mRNA translation rates. However, the underlying regulatory grammar remains elusive. Here, we propose MTtrans, a multi-task translation rate predictor capable of learning common sequence patterns from datasets across various experimental techniques. The core premise is that common motifs are more likely to be genuinely involved in translation control. MTtrans outperforms existing methods in both accuracy and the ability to capture transferable motifs across species, highlighting its strength in identifying evolutionarily conserved sequence motifs. Our independent fluorescence-activated cell sorting coupled with deep sequencing (FACS-seq) experiment validates the impact of most motifs identified by MTtrans. Additionally, we introduce “GRU-rewiring,” a technique to interpret the hidden states of the recurrent units. Gated recurrent unit (GRU)-rewiring allows us to identify regulatory element-enriched positions and examine the local effects of 5′ UTR mutations. MTtrans is a powerful tool for deciphering the translation regulatory motifs.


Persistent Identifierhttp://hdl.handle.net/10722/340777
ISSN
2023 Impact Factor: 9.0
2023 SCImago Journal Rankings: 4.872
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorZheng, Weizhong-
dc.contributor.authorFong, John H C-
dc.contributor.authorWan, Yuk Kei-
dc.contributor.authorChu, Athena H Y-
dc.contributor.authorHuang, Yuanhua-
dc.contributor.authorWong, Alan S L-
dc.contributor.authorHo, Joshua W K-
dc.date.accessioned2024-03-11T10:47:02Z-
dc.date.available2024-03-11T10:47:02Z-
dc.date.issued2023-12-20-
dc.identifier.citationCell Systems, 2023, v. 14, n. 12, p. 1103-1112-
dc.identifier.issn2405-4712-
dc.identifier.urihttp://hdl.handle.net/10722/340777-
dc.description.abstract<p>The sequence in the 5′ untranslated regions (UTRs) is known to affect mRNA translation rates. However, the underlying regulatory grammar remains elusive. Here, we propose MTtrans, a multi-task translation rate predictor capable of learning common sequence patterns from datasets across various experimental techniques. The core premise is that common motifs are more likely to be genuinely involved in translation control. MTtrans outperforms existing methods in both accuracy and the ability to capture transferable motifs across species, highlighting its strength in identifying evolutionarily conserved sequence motifs. Our independent fluorescence-activated cell sorting coupled with deep sequencing (FACS-seq) experiment validates the impact of most motifs identified by MTtrans. Additionally, we introduce “GRU-rewiring,” a technique to interpret the hidden states of the recurrent units. Gated recurrent unit (GRU)-rewiring allows us to identify regulatory element-enriched positions and examine the local effects of 5′ UTR mutations. MTtrans is a powerful tool for deciphering the translation regulatory motifs.<br></p>-
dc.languageeng-
dc.publisherElsevier-
dc.relation.ispartofCell Systems-
dc.subjecteukaryotic translation-
dc.subjectexplainable AI-
dc.subjectmotif discovery-
dc.subjectmulti-task learning-
dc.subjectsequence modeling-
dc.titleDiscovery of regulatory motifs in 5′ untranslated regions using interpretable multi-task learning models-
dc.typeArticle-
dc.identifier.doi10.1016/j.cels.2023.10.011-
dc.identifier.scopuseid_2-s2.0-85180003705-
dc.identifier.volume14-
dc.identifier.issue12-
dc.identifier.spage1103-
dc.identifier.epage1112-
dc.identifier.eissn2405-4712-
dc.identifier.isiWOS:001147492800001-
dc.identifier.issnl2405-4712-

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